EP3947529A1 - Gélatine et utilisations associées - Google Patents
Gélatine et utilisations associéesInfo
- Publication number
- EP3947529A1 EP3947529A1 EP20715390.9A EP20715390A EP3947529A1 EP 3947529 A1 EP3947529 A1 EP 3947529A1 EP 20715390 A EP20715390 A EP 20715390A EP 3947529 A1 EP3947529 A1 EP 3947529A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- gelatin
- dispensing
- present
- composition
- aqueous
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 108010010803 Gelatin Proteins 0.000 title claims abstract description 271
- 229920000159 gelatin Polymers 0.000 title claims abstract description 271
- 235000019322 gelatine Nutrition 0.000 title claims abstract description 271
- 235000011852 gelatine desserts Nutrition 0.000 title claims abstract description 271
- 239000008273 gelatin Substances 0.000 title claims abstract description 269
- 238000010146 3D printing Methods 0.000 claims abstract description 34
- 238000000034 method Methods 0.000 claims abstract description 31
- 230000008569 process Effects 0.000 claims abstract description 22
- 239000002537 cosmetic Substances 0.000 claims abstract description 16
- 239000000203 mixture Substances 0.000 claims description 115
- 238000007306 functionalization reaction Methods 0.000 claims description 22
- 239000000654 additive Substances 0.000 claims description 15
- 239000008363 phosphate buffer Substances 0.000 claims description 12
- 238000001228 spectrum Methods 0.000 claims description 12
- 239000012736 aqueous medium Substances 0.000 claims description 10
- 102000004169 proteins and genes Human genes 0.000 claims description 10
- 108090000623 proteins and genes Proteins 0.000 claims description 10
- 108091003079 Bovine Serum Albumin Proteins 0.000 claims description 9
- 229940098773 bovine serum albumin Drugs 0.000 claims description 9
- 238000012360 testing method Methods 0.000 claims description 9
- 238000004483 ATR-FTIR spectroscopy Methods 0.000 claims description 8
- 239000003814 drug Substances 0.000 claims description 8
- 238000003255 drug test Methods 0.000 claims description 8
- 239000002158 endotoxin Substances 0.000 claims description 8
- 239000004615 ingredient Substances 0.000 claims description 8
- 230000001172 regenerating effect Effects 0.000 claims description 8
- 238000007876 drug discovery Methods 0.000 claims description 7
- 239000000416 hydrocolloid Substances 0.000 claims description 7
- 239000007943 implant Substances 0.000 claims description 7
- 230000003595 spectral effect Effects 0.000 claims description 7
- 230000010261 cell growth Effects 0.000 claims description 5
- 238000010276 construction Methods 0.000 claims description 5
- 241000282414 Homo sapiens Species 0.000 claims description 4
- 241001465754 Metazoa Species 0.000 claims description 4
- 239000004067 bulking agent Substances 0.000 claims description 4
- 239000003623 enhancer Substances 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000007952 growth promoter Substances 0.000 claims description 3
- 235000015097 nutrients Nutrition 0.000 claims description 2
- 238000007639 printing Methods 0.000 abstract description 34
- 235000013305 food Nutrition 0.000 abstract description 8
- 239000000243 solution Substances 0.000 description 30
- 239000000463 material Substances 0.000 description 23
- 238000004132 cross linking Methods 0.000 description 21
- 102000008186 Collagen Human genes 0.000 description 14
- 108010035532 Collagen Proteins 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 12
- 229920001436 collagen Polymers 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 238000001879 gelation Methods 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 210000001519 tissue Anatomy 0.000 description 11
- 239000000047 product Substances 0.000 description 10
- 235000010443 alginic acid Nutrition 0.000 description 9
- 229920000615 alginic acid Polymers 0.000 description 9
- 230000008901 benefit Effects 0.000 description 8
- 239000000499 gel Substances 0.000 description 8
- 238000005259 measurement Methods 0.000 description 8
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 7
- 229940072056 alginate Drugs 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 108090000790 Enzymes Proteins 0.000 description 6
- 102000004190 Enzymes Human genes 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 229940088598 enzyme Drugs 0.000 description 6
- 210000002744 extracellular matrix Anatomy 0.000 description 6
- 238000001914 filtration Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000000523 sample Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 210000004027 cell Anatomy 0.000 description 5
- 239000003431 cross linking reagent Substances 0.000 description 5
- 230000007062 hydrolysis Effects 0.000 description 5
- 238000006460 hydrolysis reaction Methods 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 102000010834 Extracellular Matrix Proteins Human genes 0.000 description 4
- 108010037362 Extracellular Matrix Proteins Proteins 0.000 description 4
- 238000005102 attenuated total reflection Methods 0.000 description 4
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- 239000000843 powder Substances 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 3
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910001424 calcium ion Inorganic materials 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 238000011026 diafiltration Methods 0.000 description 3
- 235000012054 meals Nutrition 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000000108 ultra-filtration Methods 0.000 description 3
- 241000251468 Actinopterygii Species 0.000 description 2
- 108010088751 Albumins Proteins 0.000 description 2
- 102000009027 Albumins Human genes 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- AZKVWQKMDGGDSV-BCMRRPTOSA-N Genipin Chemical compound COC(=O)C1=CO[C@@H](O)[C@@H]2C(CO)=CC[C@H]12 AZKVWQKMDGGDSV-BCMRRPTOSA-N 0.000 description 2
- 108010025020 Nerve Growth Factor Proteins 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 108010009736 Protein Hydrolysates Proteins 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 108090000190 Thrombin Proteins 0.000 description 2
- 108060008539 Transglutaminase Proteins 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 125000003275 alpha amino acid group Chemical group 0.000 description 2
- 235000015278 beef Nutrition 0.000 description 2
- 238000005842 biochemical reaction Methods 0.000 description 2
- 239000012620 biological material Substances 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000000679 carrageenan Chemical class 0.000 description 2
- 235000010418 carrageenan Nutrition 0.000 description 2
- 229920001525 carrageenan Chemical class 0.000 description 2
- 229940113118 carrageenan Drugs 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
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- 230000002255 enzymatic effect Effects 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 235000019688 fish Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- AZKVWQKMDGGDSV-UHFFFAOYSA-N genipin Natural products COC(=O)C1=COC(O)C2C(CO)=CCC12 AZKVWQKMDGGDSV-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000017 hydrogel Substances 0.000 description 2
- 239000000411 inducer Substances 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- DCUFMVPCXCSVNP-UHFFFAOYSA-N methacrylic anhydride Chemical compound CC(=C)C(=O)OC(=O)C(C)=C DCUFMVPCXCSVNP-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 235000015277 pork Nutrition 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 229960004072 thrombin Drugs 0.000 description 2
- 102000003601 transglutaminase Human genes 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical class [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 2
- OXBLVCZKDOZZOJ-UHFFFAOYSA-N 2,3-Dihydrothiophene Chemical compound C1CC=CS1 OXBLVCZKDOZZOJ-UHFFFAOYSA-N 0.000 description 1
- SHKUUQIDMUMQQK-UHFFFAOYSA-N 2-[4-(oxiran-2-ylmethoxy)butoxymethyl]oxirane Chemical class C1OC1COCCCCOCC1CO1 SHKUUQIDMUMQQK-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 102000011690 Adiponectin Human genes 0.000 description 1
- 108010076365 Adiponectin Proteins 0.000 description 1
- 229920001817 Agar Chemical class 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 241000972773 Aulopiformes Species 0.000 description 1
- 241000283707 Capra Species 0.000 description 1
- 241000282994 Cervidae Species 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 108090000695 Cytokines Proteins 0.000 description 1
- 102000004127 Cytokines Human genes 0.000 description 1
- 238000005698 Diels-Alder reaction Methods 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- 108010014258 Elastin Proteins 0.000 description 1
- 102000016942 Elastin Human genes 0.000 description 1
- 239000004593 Epoxy Chemical class 0.000 description 1
- 241000283073 Equus caballus Species 0.000 description 1
- 108010022355 Fibroins Proteins 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 235000002918 Fraxinus excelsior Nutrition 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 244000111489 Gardenia augusta Species 0.000 description 1
- 229920002148 Gellan gum Chemical class 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- 102100039619 Granulocyte colony-stimulating factor Human genes 0.000 description 1
- 102100039620 Granulocyte-macrophage colony-stimulating factor Human genes 0.000 description 1
- 229920002907 Guar gum Chemical class 0.000 description 1
- 229920000084 Gum arabic Chemical class 0.000 description 1
- 229920000569 Gum karaya Chemical class 0.000 description 1
- 101000746367 Homo sapiens Granulocyte colony-stimulating factor Proteins 0.000 description 1
- 101000746373 Homo sapiens Granulocyte-macrophage colony-stimulating factor Proteins 0.000 description 1
- 101000599951 Homo sapiens Insulin-like growth factor I Proteins 0.000 description 1
- 102100037852 Insulin-like growth factor I Human genes 0.000 description 1
- 108010076876 Keratins Proteins 0.000 description 1
- 102000011782 Keratins Human genes 0.000 description 1
- 239000012480 LAL reagent Substances 0.000 description 1
- 241000239218 Limulus Species 0.000 description 1
- 229920000161 Locust bean gum Chemical class 0.000 description 1
- 229920002774 Maltodextrin Polymers 0.000 description 1
- 101001055320 Myxine glutinosa Insulin-like growth factor Proteins 0.000 description 1
- NQTADLQHYWFPDB-UHFFFAOYSA-N N-Hydroxysuccinimide Chemical compound ON1C(=O)CCC1=O NQTADLQHYWFPDB-UHFFFAOYSA-N 0.000 description 1
- 102000007072 Nerve Growth Factors Human genes 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
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- 229920001615 Tragacanth Chemical class 0.000 description 1
- 108090000901 Transferrin Proteins 0.000 description 1
- 102000004338 Transferrin Human genes 0.000 description 1
- 102000009618 Transforming Growth Factors Human genes 0.000 description 1
- 108010009583 Transforming Growth Factors Proteins 0.000 description 1
- 102000003425 Tyrosinase Human genes 0.000 description 1
- 108060008724 Tyrosinase Proteins 0.000 description 1
- 108010019530 Vascular Endothelial Growth Factors Proteins 0.000 description 1
- 102000005789 Vascular Endothelial Growth Factors Human genes 0.000 description 1
- 239000000205 acacia gum Chemical class 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
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- 229940041514 candida albicans extract Drugs 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 230000021164 cell adhesion Effects 0.000 description 1
- 239000001913 cellulose Chemical class 0.000 description 1
- 229920002678 cellulose Chemical class 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 238000007156 chain growth polymerization reaction Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 125000003636 chemical group Chemical group 0.000 description 1
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- 239000011248 coating agent Substances 0.000 description 1
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- 238000001816 cooling Methods 0.000 description 1
- 230000003013 cytotoxicity Effects 0.000 description 1
- 231100000135 cytotoxicity Toxicity 0.000 description 1
- AIUDWMLXCFRVDR-UHFFFAOYSA-N dimethyl 2-(3-ethyl-3-methylpentyl)propanedioate Chemical class CCC(C)(CC)CCC(C(=O)OC)C(=O)OC AIUDWMLXCFRVDR-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
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- 238000009826 distribution Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000002900 effect on cell Effects 0.000 description 1
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- 150000002334 glycols Chemical class 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
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- 239000000665 guar gum Chemical class 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
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- 230000008018 melting Effects 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920001277 pectin Chemical class 0.000 description 1
- 239000001814 pectin Chemical class 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 229960000292 pectin Drugs 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 229940066779 peptones Drugs 0.000 description 1
- 239000008055 phosphate buffer solution Substances 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000012852 risk material Substances 0.000 description 1
- 235000019515 salmon Nutrition 0.000 description 1
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- 238000004611 spectroscopical analysis Methods 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/22—Polypeptides or derivatives thereof, e.g. degradation products
- A61L27/222—Gelatin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B33—ADDITIVE MANUFACTURING TECHNOLOGY
- B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
- B33Y70/00—Materials specially adapted for additive manufacturing
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/78—Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin or cold insoluble globulin [CIG]
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
- C08H1/00—Macromolecular products derived from proteins
- C08H1/06—Macromolecular products derived from proteins derived from horn, hoofs, hair, skin or leather
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L89/00—Compositions of proteins; Compositions of derivatives thereof
- C08L89/04—Products derived from waste materials, e.g. horn, hoof or hair
- C08L89/06—Products derived from waste materials, e.g. horn, hoof or hair derived from leather or skin, e.g. gelatin
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/102—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
- C09D11/104—Polyesters
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
Definitions
- the present invention relates to a gelatin having improved properties, in particular improved dispensing properties, more particularly improved printing properties.
- the present invention further relates to a construct produced with the gelatin of the present invention and to a process to produce said construct. Further, the present invention relates to the use of the gelatin of the present invention to solve existing problems encountered with dispensing systems, in particular with 3D printing and more particularly for applications in the medical field .
- the gelatin of the present invention is particularly suitable for bio-printing in the medical field and may also be used in food applications. Background
- Dispensing techniques offer some advantages compared to standard production technologies, particularly in the medical field . Said advantages can be the speed of manufacturing, customization and the like.
- One very well-known dispensing technique is 3D printing.
- bioprinting is a powerful tool used for tissue engineering applications due to its capability of directly dispensing biological materials into spatial orientations and geometries.
- Gelatin is a preferred substrate biomaterial because of its very high biocompatibility with living tissues.
- gelatin shows a natural amino acid sequence of Arginine-Glycine-Aspartate (Arg-Gly-Asp) component which is the main amino acid sequence responsible for cell adhesion in extracellular matrices (ECMs).
- ECM extracellular matrix
- an extracellular matrix is a three- dimensional network of extracellular macromolecules, such as collagen, enzymes, and glycoproteins, that provide structural and biochemical support to surrounding cells.
- dispensing time window i.e. the time during which a material can be dispensed without showing detrimental viscosity increase upon dispensing, in particular, inside the dispensing head or nozzle. It is advantageous to have a longer dispensing time window as this gives more flexibility during the dispensing process.
- dispensing time window i.e. the time during which a material can be dispensed without showing detrimental viscosity increase upon dispensing, in particular, inside the dispensing head or nozzle.
- an important issue nowadays in dispensing technologies and particular in 3D printing the dispensing time window of materials based on gelatin is short because of the lack of thermostability. Gelatin-based formulations rapidly show an increase in viscosity after the start of the dispensing process, and this increase in viscosity causes the material to block the dispensing head.
- Dispensing can then only be done for a limited period of time before the dispensing head is blocked and has to be cleaned or changed before dispensing can be continued. This is not convenient at all to make bigger constructs or to make several smaller constructs. Thus with existing gelatin- based dispensing material, the dispensing time window is limited.
- gelatin which as mentioned above is very suitable because of its biocompatibility with living tissues, is known to be a high-risk material for nozzle clogging. Due to the thermal instability of gelatin, a gelatin solution (prepared for printing typically at concentrations above 7.5%) will rapidly show an increase in viscosity at room temperature (20 to 25 °C), and will block dispensing heads, in particular those having a diameter below 0.64 mm (or 22G).
- One solution is to dispense the material in a temperature-controlled dispensing system.
- temperature controlled systems are expensive and require great care during operation, which makes the dispensing operation quite complicated.
- Another solution is to chemically modify the dispensing material or to supplement it with additives.
- bio-printing materials include modified gelatins.
- gelatin can be mixed with other hydrocolloids such as alginates for example.
- use of only specific raw materials such as fish gelatin may be a solution.
- WO 2017216780 A1 relates to a gelatin polymer which is derived from natural sources of cold-adapted marine species, such as salmon gelatin.
- US 9 101 681 B2 relates to the use of standard gelatin to make 3D constructs in a temperature-controlled dispensing system.
- US 2015/0084232 A1 relates to hydrogel compositions for printing 3D objects, wherein the hydrogel comprises a cross-linked biocompatible polymer. Pre crosslinking is done before extrusion to ensure stability of the printing material.
- the present invention aims to solve at least the above mentioned problems.
- the present invention is based on the findings of a novel gelatin which has improved properties in particular in the field of dispensing systems (or devices), such as 3D printing systems (or devices), in particular for the medical field, in cosmetic applications and food applications, more particularly for the medical field.
- the gelatin of the present invention allows to have a longer dispensing time window, preferably printing time window, in dispensing systems, such as 3D printing systems.
- the gelatin of the present invention is thermally stable which is advantageous as it can be dispensed preferably at typical dispensing, or printing concentrations of about 7.5 to 15%, without the need of having complicated temperature controlling systems in place or the need of having complicated formulations with additives or bulking material.
- the present invention relates to a gelatin characterized in that a. It is soluble in an aqueous medium and
- the present invention relates to the gelatin of the first aspect of the present invention for use in dispensing devices, preferably 3D printing devices.
- the present invention relates to a gelatin composition
- a gelatin composition comprising the gelatin of the present invention and one or more further ingredients, from the group comprising bulking agents, hydrocolloids and proteins.
- the present invention relates to the gelatin composition of the third aspect of the present invention for use in dispensing devices, preferably 3D printing devices.
- the present invention relates to an aqueous gelatin composition comprising from 1 to 30wt% of the gelatin of the present invention or the gelatin composition of the present invention and from 70 to 99wt% of water.
- the present invention relates to the aqueous gelatin composition of the fifth aspect of the present invention for use in dispensing devices, preferably 3D printing devices.
- the present invention relates to a construct which comprises the gelatin of the present invention, or the gelatin composition of the present invention or the aqueous gelatin composition of the present invention, and wherein the gelatin is gelled.
- a construct which comprises the gelatin of the present invention, or the gelatin composition of the present invention or the aqueous gelatin composition of the present invention, and wherein the gelatin is gelled.
- said construct is produced by dispensing, preferably by 3D printing.
- the present invention relates to a process for making a construct, characterized in that it comprises the steps of
- aqueous gelatin composition in a dispensing device, preferably a 3D printer, and
- aqueous gelatin composition is according to the present invention.
- the present invention relates to the use of the gelatin of the present invention or of the gelatin composition of the present invention, or of the aqueous gelatin composition of the present invention to increase the dispensing time window in dispensing systems, preferably to increase the printability time window in 3D printing systems.
- the present invention relates to the use of the gelatin of the present invention or of the gelatin composition of the present invention, or of the aqueous gelatin composition of the present invention to obtain a dispensing time window in dispensing devices as defined above, preferably a printing time window in 3D printing devices, of from above 15 minutes to 3 hours, more preferably from 20 minutes to 2 hours and 30 minutes, even more preferably from 30 minutes to 2 hours, yet even more preferably from 40 minutes to 2 hours, yet even more preferably from 40 minutes to 2 hours, yet even more preferably from 50 minutes to 2 hours, yet even more preferably from 1 hour to 2 hours.
- the present invention relates to the use of the gelatin of the present invention, or of the gelatin composition of the present invention or of the aqueous gelatin composition of the present invention to reduce or delay the clogging of dispensing systems during dispensing process, preferably to reduce or delay the clogging of 3D printing systems during 3D printing process.
- the present invention relates to the use of the gelatin of the present invention, or of the gelatin composition of the present invention or of the aqueous gelatin composition of the present invention in the production of scaffolds, engineered tissues, devices or micro-devices suitable for therapeutic purposes, diagnostic purposes, research purposes and the like, said production being done by dispensing, preferably by 3D printing.
- the present invention relates to the use of the construct of the present invention as a scaffold for tissue engineering, for regenerative medicine, for diagnostic purposes, for drug testing and the like.
- gelatin refers to its well-known definition in the art, i.e. it is a linear polymer resulting from partial hydrolysis of collagen. Said partial hydrolysis may be obtained by chemical, enzymatic and/or heat treatment of collagen. In the case of gelatin, hydrolysis of collagen is said to be partial because gelatin keeps some functional properties (such as the ability to form gels) contrary to collagen hydrolysate, which have lost such functional properties of forming gels.
- Gelatin may be derived from collagen sourced of any suitable type of connective animal tissue, particularly from bones, teeth and hides, preferably collagen is sourced from bones and/or hides.
- Collagen may be derived from different animals such as pork, beef, sheep, goat, horse, deer, chicken, fish and the like.
- collagen and thus also gelatin is derived from pork and/or beef.
- Standard gelatin requires to be heated in order to dissolve in water.
- standard gelatin forms a gel, the strength of said gel depends on the specific properties of the gelatin such as molecular weight distribution and molecular conformation.
- Gelatin is mostly characterized by its gel strength, expressed in g Bloom. Further, gelatin is also characterized by a certain viscosity, expressed in mPa.s. Among others, further properties of gelatin are bulk weight or bulk density and particle size.
- dispenser systems or “dispensing devices” refer to apparatus able to deposit a composition, typically as a liquid or paste, onto a surface in the form of dots, lines and any other suitable shapes.
- a composition typically as a liquid or paste
- said composition is pushed from a reservoir onto a surface through a head, which is typically a nozzle.
- the head may be driven by pressure, piezoelectric motor or laser- assisted jetting.
- the head may be of different sizes and different openings, also the need for more or less pressure will depend on the apparatus and composition to be dispensed.
- Dispensing may be done by extrusion, spraying, jetting and the like.
- Dispensing devices are preferably computer- controlled systems. A suitable software allows the user to enter a pre-determined shape which is then dispensed on a surface by the dispensing device to provide a construct.
- a dispensing device may be a 3D printer, an ink jet printer, a single jet dispensing device, and the like.
- the dispensing device is a 3D printing system, i.e. a 3D printer.
- dispensing comprises 3D printing.
- 3D printing refers to a specific dispensing system. 3D printing systems allow to produce tridimensional shaped products, typically by depositing a composition layer by layer until the desired shape is obtained. 3D printing is, as many other dispensing systems, a computer-controlled system. Preferably in the present invention, 3D printing systems do not require temperature control during printing.
- dispensing time window refers to the time during which the composition to be dispensed can be dispensed without encountering dispensing problems due to, for example, the change in rheology of the composition within the reservoir and/or through the dispensing head of the dispensing system.
- the dispensing time window starts when dispensing begins and ends when the dispensing head gets clogged by the composition or when the dispensing does no longer happen in a suitable, uniform manner, e.g. undesired lumps are formed, dispensing spots are missed and the like, which is disturbing the desired final shape of the construct.
- crosslinking refers to the formation of a stable network structure, in particular stable network gel structure, via covalent bonding.
- crosslinking is obtained by the action of an external factor (crosslinking factor) such as exposure to heat, exposure to UV light (photo-initiated chain-growth polymerization or crosslinking) and the like, on functionalized molecules.
- an external factor such as exposure to heat, exposure to UV light (photo-initiated chain-growth polymerization or crosslinking) and the like.
- functionalized molecules are first functionalized such that crosslinking can happen upon subjection to the right conditions.
- functional groups are added to the chemical structure of (some of) the molecules by a chemical reaction (chemical functionalization) or by a biochemical reaction (biochemical functionalization) such as an enzymatic reaction for example (enzymatic functionalization).
- Chemical functionalization may be for example an acrylation reaction, i .e. introducing acrylate substitution groups; a methacrylation reaction, i.e. introducing methacrylate substitution groups, diels -alder, azide-alkyne cycloaddition reaction, thiol-ene chemistry (click chemistry) or a succinylation reaction.
- acrylation reaction i .e. introducing acrylate substitution groups
- methacrylation reaction i.e. introducing methacrylate substitution groups, diels -alder, azide-alkyne cycloaddition reaction, thiol-ene chemistry (click chemistry) or a succinylation reaction.
- Other chemical or biochemical functionalizations are not excluded.
- Molecules may also be previously treated to add reactive groups in their chemical structure in order to give access to new functional chemical groups which will facilitate crosslinking.
- crosslinking may also be obtained for example by the reaction of certain components present in a composition with specific reactants, for example, alginate present in a composition will react and crosslink when exposed to calcium ions, for example when the composition is put in a bath comprising calcium ions.
- alginate present in a composition will react and crosslink when exposed to calcium ions, for example when the composition is put in a bath comprising calcium ions.
- a composition to be crosslinked it is sufficient that at least one of its components is crosslinked.
- a composition comprising gelatin and alginate may be crosslinked when it is exposed to calcium ions, in that case only the alginate is in fact crosslinked, however it may be said that the composition is crosslinked.
- crosslinkable refers to the ability of a composition to react to an external crosslinking factor causing at least two components of the composition to be crosslinked.
- a composition can be made crosslinkable by adding functional groups to the chemical structure of (some of) the component(s) of the composition by a chemical or biochemical reaction (see above: functionalization).
- a composition can be made crosslinkable by adding crosslinking agents (or crosslinking inducers) such as formaldehyde, glutaraldehyde, l-ethyl-3-(3-dimethylaminopropyl), carbodiimide/N-hydroxysuccinimide, 1,4- Butanediol Diglycidyl Ether, epoxy compounds and the like.
- Natural crosslinking agents are for example enzymes (for example transglutaminase) and genipin (an agent extracted from gardenia fruit). Such natural crosslinking agents can provide lower cytotoxicity levels.
- Crosslinking agents like e.g. genipin containing more than one reactive group may react with reactive groups on more than one protein molecule and chemically crosslink the gelatin molecules; the crosslink inducers then become part of the crosslinked structure chemically.
- Enzymes, e.g. transglutaminases or tyrosinases catalyse the chemical reaction between reactive groups on the protein molecule to form chemical bonds and inter- and intra molecular crosslinks; the enzyme does not become part of the crosslinked network chemically.
- the invention will further be illustrated with different embodiments. It is understood that, unless expressly mentioned, all embodiments/aspects may be combined with one another.
- the present invention relates to a gelatin characterized in that a. it is soluble in an aqueous medium and
- the first derivative of the gelatin's FTIR-ATR spectrum remains below zero within the 1440-1355 cm -1 spectral region.
- the gelatin comprises from 95 weight% (wt%) to 100wt%, preferably at least 96wt%, more preferably at least 97wt%, yet even more preferably at least 98wt%, yet even more preferably at least 99wt% of gelatin on dry basis of gelatin (wt% db).
- the gelatin may indeed comprise some minor amounts of ashes and/or salts which typically result from the processing of collagen into gelatin.
- the gelatin of the present invention is soluble in an aqueous medium.
- solubility in an aqueous medium means that when lOg of the gelatin is stirred in 100ml of demi-water at 60°C during lhour, a clear solution is obtained with no particles visible to the naked eye.
- FTIR is a well-known method to characterize the structure of organic components.
- the FTIR-ATR spectrum of a gelatin sample is obtained with a resolution of 4 cm -1 , accumulating 16 scans per spectrum. Spectral measurements are performed within the mid-infrared range of 4500-600 cm -1 . Measurement is performed with a diamond triple-bounce ATR accessory (Bruker, Tensor 27). Background air spectrum is collected before each sample measurement. A sample is directly compressed on attenuated total reflectance (ATR) crystal prior to analysis without any preliminary preparation. After measurement of a gelatin sample, ethanol and distilled water are used to clean the diamond ATR crystal, which has to dry before performing a next measurement. Between each sample measurement a blank measurement is done (i.e. measurement without presence of sample). The spectra is depicted in transmittance mode.
- OriginPro8.5 is used to calculate the first derivative of the spectra within the 1440 - 1355 cm-1 wavenumber range.
- the signal is smoothed by applying a quadratic Savitzky-Golay filter with 5-points.
- the gelatin of the present invention may be obtained by a process of flash hydrolysis followed by rapid evaporation of water.
- the gelatin is further characterized in that it shows a shift of the peak in the region of the C-N-H bending band (1565-1500 cm -1 ) of about 9 cm -1 , preferably of about 7 cm 1 , more preferably about 5 cm 1 towards the lower ranges of wavenumber, compared to the gelatin starting material.
- the gelatin is in powder form, particle size may vary but is preferably 70 to 8 mesh, more preferably 60 to 15 mesh, even more preferably 60 to 20 mesh, yet even more preferably 50 to 30 mesh, yet even more preferably 40 to 30 mesh.
- the gelatin has a gel strength of above 50g Bloom, preferably from 50g to 360g Bloom, preferably 80g to 350g Bloom, more preferably lOOg to 350g Bloom, yet even more preferably 120g to 340g Bloom, yet even more preferably 150g to 340g Bloom, yet even more preferably 180g to 330g Bloom, yet even more preferably 200g to 330g Bloom, yet even more preferably 250g to 330g Bloom, yet even more preferably 270g to 320g Bloom, yet even more preferably 280g to 320g Bloom.
- a gel strength of above 50g Bloom preferably from 50g to 360g Bloom, preferably 80g to 350g Bloom, more preferably lOOg to 350g Bloom, yet even more preferably 120g to 340g Bloom, yet even more preferably 150g to 340g Bloom, yet even more preferably 180g to 330g Bloom, yet even more preferably 200g to 330g Bloom, yet even more preferably 250g to 330g Bloom, yet even more preferably 270g to
- the gelatin of the present invention is substantially not functionalized.
- substantially not functionalized means that the degree of functionalization, in particular the degree of chemical functionalization is less than 5%, more preferably from 3% to 0%, yet even more preferably from 1% to 0%, most more preferably from 0.1% to 0%.
- Functionalization is as defined above.
- the gelatin of the present invention is functionalized, meaning that the gelatin of the present invention is subjected to a functionalization reaction.
- Functionalization is as defined above. It is an advantage of the present gelatin that due to its high amounts of gelatin, a functionalization reaction is easier to perform, compared to other dispensing material where the composition renders a functionalization reaction more difficult to perform, or makes it more difficult to find the right reaction conditions.
- the degree of functionalization is from 30% to 95%, more preferably from 35 to 90%, yet even more preferably from 40 to 85%, yet even more preferably from 45 to 80%, yet even more preferably from 50 to 75%, yet even more preferably from 55 to 70%, yet even more preferably from 60 to 65%.
- the gelatin is chemically functionalized, more preferably the gelatin is acrylated or methacrylated, more preferably the gelatin is methacrylated.
- the present invention further relates to a functionalized gelatin, preferably a methacrylated gelatin characterized in that it is prepared by providing a gelatin according to the present invention and subjecting the gelatin of the present invention to a functionalization reaction, preferably to a methacrylation reaction.
- the gelatin comprises functionalized gelatin of the present invention and substantially non functionalized gelatin of the present invention.
- the gelatin comprises functionalized gelatin of the present invention and substantially non functionalized gelatin of the present invention.
- from 1 to 99wt%, preferably from 5 to 90wt%, more preferably from 10 to 80wt%, even more preferably from 20 to 60wt%, yet even more preferably from 30 to 50wt% yet even more preferably from 40 to 50wt% of the gelatin is functionalized and from 1 to 99wt%, preferably from 5 to 90wt%, more preferably from 10 to 80wt%, even more preferably from 20 to 60wt%, yet even more preferably from 30 to 50wt% yet even more preferably from 40 to 50wt% is substantially not functionalized.
- the degree of functionalization is as described here above.
- methacrylate groups are introduced on the gelatin molecules through a well-known process: typically gelatin is dissolved in a solvent, typically phosphate buffer saline (PBS) or dimethyl sulfoxide solvent (DMSO), methacrylic anhydride is then directly added to said gelatin solution, the methacrylation reaction is conducted at about 50°C.
- PBS phosphate buffer saline
- DMSO dimethyl sulfoxide solvent
- the degree of methacylation can be controlled by the amount of methacrylic anhydride added.
- the gelatin of the present invention may be methacrylated and may have a degree of methacrylation as mentioned above.
- the gelatin of the present invention comprises less than 100 Endotoxin Units (EU), more preferably less than 80 EU, even more preferably less than 60 EU, yet even more preferably less than 40 EU, yet even more preferably less than 30 EU, yet even more preferably less than 10 EU per gram of gelatin, expressed on as is basis.
- Endotoxins may be removed by clearance filters for endotoxins removal such as charged filters.
- Such charged filters are available and can be for example Mustang E ® membrane and Mustang Q ® membrane (from Pall), Sartobind ® filter (from Sartorious).
- the LAL test (acronym for Limulus Amebocyte Lysate) is a test for the determination of bacterial endotoxins, which uses an Amebocyte Lysate of the Limulus crab.
- the gelatin of the present invention is purified by using one or more of the following techniques: ultrafiltration, diafiltration, filtration with depth filters. These filtration techniques are useful to (partially) remove for example undesired toxins, bacteria, product fractions and the like.
- the gelatin of the present invention comprises 5wt% or less than 5wt%, more preferably 4wt% or less than 4wt%, even more preferably 3wt% or less than 3wt%, yet even more preferably 2wt% or less than 2wt%, yet even more preferably lwt% or less than lwt%, yet even more preferably 0.5wt% or less than 0.5wt%, yet even more preferably 0.1wt% or less than 0.1wt% of additives, on dry basis of the gelatin. More preferably, the gelatin of the present invention comprises substantially no additives.
- Additives may be rheological enhancers, flowability enhancers and the like, such as for example glycols, starches, alginates and the like. It is an advantage of the present gelatin to comprises such low amounts of additives in the ranges mentioned above, in particularly to comprise substantially no additives, in particular when the gelatin is used to produce scaffolds for use as ECM with living cells as the additives have a negative effect on cell survival rates.
- Many current material for producing scaffolds for use as ECM nowadays comprise additives in order to allow the materials to be dispensed, in particular to be 3D printed into said scaffolds.
- said solution keeps a substantially consistent flow behavior for at least 15 minutes. Dispensing is to be done at most 3hours after preparation of said solution.
- the solution is prepared by dissolving gelatin at 50°C for 30minutes after which the solution may be returned to room temperature (18 to 25°C, preferably 20 to 25°C).
- dispensing is done at around the gelation temperature of the 10% solution of gelatin, i.e. at a temperature in the range of about 10°C less to 10°C more than the gelation temperature, preferably 5°C less to 5°C more than the gelation temperature.
- the possibility to print at said temperature is an advantage of the present invention, indeed, existing gelatin-based printing material cannot be printed at a temperature around the gelation temperature unless specific measures are taken such as for example the addition of specific additives.
- existing gelatin-based printing material are often printed in heated system, more than at least 10°C, at least 15°C or even at least 20°C above the gelation temperature.
- dispensing can be done at lower pressure with the gelatin of the present invention, compared to existing gelatin- based printing material.
- said solution keeps a substantially consistent flow behavior for a time of from above 15 minutes to 3 hours, more preferably from 20 minutes to 2 hours and 30 minutes, even more preferably from 30 minutes to 2 hours, yet even more preferably from 40 minutes to 2 hours, yet even more preferably from 40 minutes to 2 hours, yet even more preferably from 50 minutes to 2 hours, yet even more preferably from 1 hour to 2 hours.
- the present invention relates to the gelatin of the first aspect of the present invention for use in dispensing devices, preferably for use in a 3D printer. It has been found that said gelatin is particularly suitable for dispensing, in particular for 3D printing, such as for use as a bio-ink in 3D printing.
- the present invention also relates to the gelatin of the first aspect of the present invention for use in the construction of scaffold for medical applications, preferably for tissue engineering, for regenerative medicine, for implants, for medical devices, for drug discovery and drug testing; or for cosmetic applications, preferably a scaffold for testing of cosmetic products; and the like.
- the gelatin can be dispensed, without the need of having a temperature controlled dispensing system and without the need of having other ingredients added, or additives added or other solutions that are typically used in the art to be able to dispense gelatin.
- Preferably dispensing is done under pressure, more preferably at room temperature.
- Dispensing, and particularly printing is done by putting the material into an aqueous solution.
- the solvent may be a phosphate buffer, bovine serum albumin (BSA), water, preferably the solvent is a phosphate buffer or BSA, more preferably a phosphate buffer.
- the gelatin is put in solution at a temperature of from 30 to 60°C, more preferably from 40 to 55°C, yet even more preferably from 40 to 50°C and allowed to cool down to room temperature before dispensing. It is preferable to start the dispensing process before a period of maximum 3 hours after cool down.
- the gelatin of the present invention is used in dispensing devices as a solution comprising from 1 to 30wt%, more preferably from 5 to 25wt%, even more preferably from 7.5 to 20wt%, yet even more preferably from 7.5 to 15wt%, yet even more preferably from 10 to 15wt% of the gelatin of the present invention.
- the present invention relates to a gelatin composition
- a gelatin composition comprising the gelatin of the first aspect of the present invention and further ingredients.
- gelatin composition is in powder form.
- the gelatin composition comprises one or more further ingredients chosen from bulking agents, hydrocolloids, proteins, anticaking agents and the like.
- the gelatin composition of the present invention comprises from 40wt% to 95wt%, more preferably from 45wt% to 95wt%, even more preferably from 50wt% to 95wt%, yet even more preferably from 55wt% to 95wt%, yet even more preferably from 60wt% to 95wt%, yet even more preferably from 65wt% to 95wt%, yet even more preferably from 70wt% to 95wt%, yet even more preferably from 75wt% to 95wt%, yet even more preferably from 80wt% to 95wt%, yet even more preferably from 85wt% to 95wt% of the gelatin of the present invention, on dry basis of the gelatin composition.
- the gelatin composition of the present invention comprises from 5wt% to 60wt%, more preferably from 5wt% to 55wt%, even more preferably from 5wt% to 50wt%, yet even more preferably from 5wt% to 45wt%, yet even more preferably from 5wt% to 40wt%, yet even more preferably from 5wt% to 35wt%, yet even more preferably from 5wt% to 30wt%, yet even more preferably from 5wt% to 25wt%, yet even more preferably from 5wt% to 20wt%, yet even more preferably from 5wt% to 15wt% of the further ingredients as defined herein.
- Bulking agents are well-known in the art and refer to material which do not possess any functionality, inert products, such as sugars, mono-, di- and tri-saccharides, maltodextrins, fibers, protein hydrolysates (such as collagen hydrolysates for example) and the like.
- Hydrocolloids may be one or more of alginate, pectin, carrageenan, gellan, agar, starch, xanthan gum, locust bean gum, guar gum, gum karaya, gum tragacanth, gum Arabic, cellulose derivatives, chitosan and the like.
- the hydrocolloids are alginate or carrageenan, more preferably alginate.
- Proteins may be one or more of keratin, elastin, fibroin, thrombin, albumin, and the like. Protein may also be derived from collagen raw materials.
- the gelatin composition comprises functionalized gelatin of the present invention and regular gelatin (i.e. not according to the present invention) which is not functionalized.
- the gelatin composition preferably comprises from 1 to 99wt%, preferably from 5 to 90wt%, more preferably from 10 to 80wt%, even more preferably from 20 to 60wt%, yet even more preferably from 30 to 50wt% yet even more preferably from 40 to 50wt% of functionalized gelatin of the present invention (the degree of functionalization is as described above), and from 1 to 99wt%, preferably from 5 to 90wt%, more preferably from 10 to 80wt%, even more preferably from 20 to 60wt%, yet even more preferably from 30 to 50wt% yet even more preferably from 40 to 50wt% of regular gelatin, non-functionalized.
- the gelatin composition of the present invention has been purified by using one or more of the following techniques: ultrafiltration, diafiltration, filtration with depth filters. These filtration techniques are useful to remove or at least substantially lower the amount of bacteria, endotoxins, fats, non-collagen proteins, fibres and the like.
- the present invention relates to the gelatin composition of the third aspect of the present invention for use in dispensing devices, preferably in 3D printer. It has been found that said gelatin composition is particularly suitable for dispensing, in particular 3D printing, such as for use as a bio-ink in 3D printing.
- the present invention also relates to the gelatin composition of the third aspect of the present invention for use in the construction of scaffold for medical applications, preferably for tissue engineering, for regenerative medicine, for implants, for drug discovery and drug testing, or for cosmetic applications, preferably a scaffold for testing of cosmetic products and the like, or for food applications, such as for example personalized meals, reconstituted meals and the like.
- the gelatin composition can be dispensed when put into solution without the need of having a temperature-controlled dispensing system and without the need of having additives added or other solutions that are typically used in the art to be able to dispense gelatin composition.
- Preferably dispensing is done under pressure, more preferably at room temperature.
- Dispensing, and particularly printing is done with the gelatin composition put into an aqueous solution.
- the solvent may be a phosphate buffer, BSA, water, preferably it is a phosphate buffer or BSA, more preferably a phosphate buffer.
- the gelatin composition is put in solution at a temperature of from 30 to 60°C, more preferably from 40 to 55°C, yet even more preferably from 40 to 50°C and allowed to cool down to room temperature before dispensing. It is preferable to start the dispensing process maximum before a period of 3 hours after cool down.
- a further advantage of the present gelatin composition is that it can be dispensed as a highly concentrated aqueous solution, i.e. aqueous solution containing up to 30wt% of the gelatin composition, preferably the present gelatin composition is used in dispensing devices as a solution comprising from 1 to 30wt%, more preferably from 5 to 25wt%, even more preferably from 7.5 to 20wt%, yet even more preferably from 7.5 to 15wt%, yet even more preferably from 10 to 15wt% of the gelatin of the present invention.
- the present invention relates to an aqueous gelatin composition
- an aqueous gelatin composition comprising from 1 to 30wt%, preferably from 5 to 25wt%, even more preferably from 7.5 to 20wt%, yet even more preferably from 7.5 to 15wt%, yet even more preferably from 10 to 15wt% of the gelatin of the first or second aspect of the present invention or of the third or fourth aspect of the present invention and from 70 to 99wt%, preferably from 95 to 75wt%, even more preferably from 80 to 92.5wt%, yet even more preferably from 85 to 92.5wt%, yet even more preferably from 85 to 90wt% of an aqueous medium.
- the aqueous medium may be a phosphate buffer, bovine serum albumin (BSA), water, preferably the solvent is a phosphate buffer or BSA, more preferably a phosphate buffer.
- the aqueous gelatin composition of the present invention comprises various components, preferably cell growth components, i.e. components which have a beneficial effect on the growth of living plant, human or animal cells.
- Such components may be cytokines (Adiponectin Human) cell growth promoters or growth factors, such as (EGF, FGF, NGF, PDGF, VEGF, IGF, GMCSF, GCSF, TGF, Erythropieitn, TPO, BMP, HGF, GDF, Neurotrophins, MSF, SGF, GDF); nutrients, such as glucose, yeast extract; salts, such as potassium chloride, sodium chloride and the like; proteins, such as thrombin transferrin, albumin, peptones and the like.
- cytokines Adiponectin Human
- growth factors such as (EGF, FGF, NGF, PDGF, VEGF, IGF, GMCSF, GCSF, TGF, Erythropieitn, TPO, BMP, HGF,
- the aqueous gelatin composition of the present invention further comprises living organisms, preferably human, animal and/or plant cells. Said living organisms may be encapsulated or non-encapsulated.
- the aqueous gelatin composition of the present invention is prepared by bringing all components in solution at a temperature of from 30 to 60°C, preferably from 40 to 55°C, yet even more preferably from 40 to 50°C and letting the aqueous composition cool down to room temperature before further use.
- the aqueous gelatin composition of the present invention has been purified by using one or more of the following techniques: ultrafiltration, diafiltration, filtration with depth filters. These filtration techniques are useful to remove or at least substantially lower the amount of bacteria, endotoxins (removal of e.g. from 10 to 90% of endotoxins), fats, non-collagen proteins, fibres and the like.
- the present invention relates to the aqueous gelatin composition of the present invention for use in dispensing devices, preferably in 3D printer. It has been found that said aqueous gelatin composition is particularly suitable for dispensing, in particular for use as a bio-ink in 3D printing.
- the present invention also relates to the aqueous gelatin composition of the present invention for use in dispensing devises, preferably in 3D printers, in the construction of scaffold for medical applications, preferably for tissue engineering, for regenerative medicine, for implants, for drug discovery and drug testing, or for cosmetic applications, preferably a scaffold for testing of cosmetic products, or food applications and the like. Also the present aqueous gelatin composition is very suitable for dispensing, preferably 3D printing.
- the aqueous gelatin composition can be dispensed without the need of having a temperature-controlled dispensing system and without the need of having additives added or other solutions that are typically used in the art to be able to dispense aqueous gelatin compositions.
- Preferably dispensing is done under pressure, more preferably at room temperature.
- the aqueous gelatin composition is heated to a temperature of from 30 to 60°C, more preferably from 40 to 55°C, yet even more preferably from 40 to 50°C and allowed to cool down before dispensing. It is not desired to keep the cooled aqueous gelatin composition for a period of time of more than 3hours at room temperature before starting the dispensing process.
- the present invention relates to a construct, comprising the gelatin of the present invention, the gelatin composition of the present invention and/or the aqueous gelatin composition of the present invention, wherein the gelatin is gelled.
- a construct comprising the gelatin of the present invention, the gelatin composition of the present invention and/or the aqueous gelatin composition of the present invention, wherein the gelatin is gelled.
- said construct being produced by dispensing, more preferably by 3D printing.
- the gelatin of the present invention may or may not be functionalized.
- the construct is crosslinkable, and crosslinking may be done by application of the right crosslinking conditions (such as applying a photoinitiator for example).
- crosslinking reaction has been performed, it may be said that the construct is crosslinked.
- Crosslinked constructs especially comprising gelatin which is a natural ingredient that melts at body temperature, are very stable and can be introduced in the body or used at temperatures above the melting temperature of gelatin, without the fear that the construct would melt away or show deformations.
- crosslinking takes place immediately after dispensing (filament deposition) to ensure self-supporting properties of the 3D-construct, to avoid collapsing of the 3D construct after printing.
- the construct may further comprise one or more of other components such as carbohydrates, salts, living cells, cell growth promoters and enzymes.
- the construct may comprise the gelatin, the gelatin composition and/or the aqueous gelatin composition of the present invention ('gelatin comprising compositions') and other further components due to for example dispensing the construct with multiple headed nozzles, where one or more nozzles dispensing the gelatin comprising composition and the other one or more nozzles dispensing another type of suitable composition which can be dispensed and is preferably biocompatible, such as a composition comprising hydrocolloids, for example, alginate; proteins; carbohydrates and the like.
- the present invention relates to a process for making a construct, characterized in that the process comprises the steps of
- aqueous gelatin composition in a dispensing device, preferably a 3D printer, and
- aqueous gelatin composition is according to the present invention.
- the construct is as defined herein.
- Operating the dispensing device may be done at a controlled temperature such as at a temperature of from above 25 to 40°C, however advantageously with the present aqueous gelatin composition, dispensing is done without controlled temperature system, at room temperature (18 to 25°C, preferably 20 to 25°C).
- dispensing is is done at around the gelation temperature of the 10% solution of gelatin, i.e. at a temperature in the range of about 10°C less to 10°C more than the gelation temperature, preferably 5°C less to 5°C more than the gelation temperature.
- the construct is made by dispensing, preferably by printing, layer above layer or dot above dot of the aqueous gelatin composition. If needed the construct may also be a single layer or dot of the aqueous gelatin composition. In fact, any suitable construct may be printed, in accordance with the possibilities of the used dispensing system, preferably of the used 3D printer software.
- the construct may be crosslinked, provided either that the aqueous gelatin composition was functionalized to be crosslinked or provided that enzymes have been added which can cause crosslinking.
- crosslinking takes place right after dispensing (filament deposition), i.e. the moment of cross-linking depending on the viscoelastic properties of the dispended material, to ensure self- supporting properties of the 3D-construct, thus cross-linking is done on time after dispensing to avoid collapsing of the 3D construct after dispensing or printing.
- thermostability of the gelatin of the present invention is advantageous as it allows to prevent the combined effect of physical gel formation together with increments of viscosity caused by (chemical) crosslinking, making it possible to have a more flexible time control during dispensing process.
- the present invention further relates to the use of the gelatin of the present invention, the gelatin composition of the present invention or the aqueous gelatin composition of the present invention to increase the dispensing time window in dispensing systems, preferably to increase the printability time window in 3D printing systems.
- gelatin, gelatin composition and aqueous gelatin compositions show little to no viscosity increase during printing, also at room temperature, in fact even at around the gelation temperature of the gelatin, as defined above , for a period of time of up to 3 hours, preferably of above 15 minutes to 3 hours, more preferably from 20 minutes to 2 hours and 30 minutes, even more preferably from 30 minutes to 2 hours, yet even more preferably from 40 minutes to 1 hour and 30 minutes, yet even more preferably from 40 minutes to 1 hour.
- previous compositions comprising gelatin typically only allowed a dispensing time window of about 15 minutes or less.
- clogging of the dispensing head or nozzle, preferably printing nozzle does not happen until after 3 hours of dispensing, preferably printing, preferably not until after a period of above 15 minutes to 3 hours, more preferably from 20 minutes to 2 hours and 30 minutes, even more preferably from 30 minutes to 2 hours, yet even more preferably from 40 minutes to 2 hours, yet even more preferably from 40 minutes to 2 hours, yet even more preferably from 50 minutes to 2 hours, yet even more preferably from 1 hour to 2 hours.
- the present invention relates to the use of the gelatin, gelatin composition and aqueous gelatin compositions of the present invention in the preparation, preferably by dispensing, more preferably by 3D printing, of a scaffold for medical applications, preferably for tissue engineering, for regenerative medicine, for implants, for drug discovery and drug testing, or for cosmetic applications, preferably a scaffold for testing of cosmetic products, and the like.
- a scaffold for medical applications preferably for tissue engineering, for regenerative medicine, for implants, for drug discovery and drug testing, or for cosmetic applications, preferably a scaffold for testing of cosmetic products, and the like.
- the present invention relates to the use of the gelatin, gelatin composition and aqueous gelatin compositions of the present invention in the preparation of food applications such as customized meals, reconstituted foods, bakery applications and the like.
- the present invention relates to the use of the construct of the present invention in the preparation of a scaffold for medical applications, preferably for tissue engineering, for regenerative medicine, for implants, for drug discovery and drug testing, or for cosmetic applications, preferably a scaffold for testing of cosmetic products, and the like.
- the present invention relates to a process for identifying a gelatin suitable for use in dispensing device, preferably for use in 3D-printing devices, said process comprises the steps
- said gelatin is suitable for use in said dispensing device when the first derivative of the gelatin's FTIR-ATR spectrum remains below zero within the 1440-1355 cm -1 spectral region and the gelatin is soluble in aqueous medium.
- Fig 1 a, b and c exemplify the difference between printability and non-printability.
- the composition is not printable as there is no shape fidelity.
- Fig lb it can be seen that the composition is printable, it has a good consistency for extrusion-based 3D printers.
- Fig lc it can be seen that the composition is not printable due to clogging of the nozzle causing disturbance in shape of the construct, the experiment required pausing of the printing job for nozzle replacement.
- Example 1 production of gelatin according to the present invention
- the heated gelatin is then submitted to evaporation by roll-coating the heated gelatin solution on the surface of a rotating cylinder heated by steam at 4.5 bar.
- the adhering thin layer of product on the surface of the cylinder is rapidly dried and scratched off by the action of a sharp knife.
- the gelatin so produced is soluble in water.
- the FTIR-ATR spectrum of the gelatin so produced is measured.
- the first derivative and the transmittance is depicted in figure 2 (3).
- the first derivative of the spectrum of the gelatin of the present invention remains below zero within the 1440-1355 cm -1 spectral region.
- the 2 syringes are placed on the bench and allowed to cool at ambient temperature conditions (about 20°C).
- the syringe containing the gelatin according to example 1 is placed in the print- head 1 (PHI) and the syringe containing the regular gelatin is placed in the print- head 2 (PH2).
- PHI print- head 1
- PH2 print- head 2
- Printing of 6 lattice structures was initiated simultaneously by PHI and PH2.
- the printing settings applied on the Slic3r software for printing of a lattice structure are adjusted as follows:
- the gelatin according to example 1 requires extrusion pressure of 85-100kPa while the regular gelatin requires a pressure of 130-140kPa in order to have filament formation.
- the printing of a third lattice construct is not possible due to complete blockage of the nozzle.
- the gelatin according to example 1 it is possible to print up to 6 lattice constructs, printing can be done up to 105 minutes without any blockage of the nozzle and uniform filament production, the flow behavior remains uniform during the entire printing operation.
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Abstract
La présente invention concerne une gélatine possédant des propriétés améliorées, notamment des propriétés de distribution améliorées, et plus particulièrement des propriétés d'impression améliorées. La présente invention concerne en outre une construction produite avec la gélatine de la présente invention et un procédé de production de ladite construction. En outre, la présente invention concerne l'utilisation de la gélatine de la présente invention pour résoudre des problèmes existants rencontrés avec des systèmes de distribution, en particulier avec une impression 3D et plus particulièrement pour des applications dans le domaine médical. La gélatine de la présente invention est particulièrement appropriée pour une bio-impression dans le domaine médical et peut également être utilisée dans des applications cosmétiques et dans des applications alimentaires.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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EP19167094.2A EP3719057A1 (fr) | 2019-04-03 | 2019-04-03 | Gélatine et ses utilisations |
PCT/EP2020/059669 WO2020201555A1 (fr) | 2019-04-03 | 2020-04-03 | Gélatine et utilisations associées |
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EP3947529A1 true EP3947529A1 (fr) | 2022-02-09 |
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EP19167094.2A Withdrawn EP3719057A1 (fr) | 2019-04-03 | 2019-04-03 | Gélatine et ses utilisations |
EP20715390.9A Pending EP3947529A1 (fr) | 2019-04-03 | 2020-04-03 | Gélatine et utilisations associées |
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EP19167094.2A Withdrawn EP3719057A1 (fr) | 2019-04-03 | 2019-04-03 | Gélatine et ses utilisations |
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US (1) | US20220184274A1 (fr) |
EP (2) | EP3719057A1 (fr) |
JP (1) | JP2022527533A (fr) |
CN (1) | CN113677742A (fr) |
CA (1) | CA3135934A1 (fr) |
IL (1) | IL286899A (fr) |
MX (1) | MX2021012139A (fr) |
WO (1) | WO2020201555A1 (fr) |
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KR102493622B1 (ko) * | 2020-10-16 | 2023-01-31 | 주식회사 파이버엔텍 | 고강도 콜라겐 필라멘트의 제조방법 |
CN113683789B (zh) * | 2021-08-19 | 2022-04-29 | 江南大学 | 一种3d打印水凝胶及其制备方法 |
CN113999405B (zh) * | 2021-10-29 | 2024-01-30 | 广东省科学院健康医学研究所 | 一种明胶复合水凝胶及其制备方法 |
Family Cites Families (8)
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US8753672B2 (en) * | 2006-04-24 | 2014-06-17 | Coloplast A/S | Gelatin non-woven structures produced by a non-toxic dry solvent spinning process |
EP1961411A1 (fr) * | 2007-02-21 | 2008-08-27 | FUJIFILM Manufacturing Europe B.V. | Composition de libération contrôlée |
US9169521B1 (en) * | 2013-03-14 | 2015-10-27 | The Boeing Company | Point-of-collection sample preparation device and method |
US10173357B2 (en) * | 2013-09-26 | 2019-01-08 | Northwestern University | Poly(ethylene glycol) cross-linking of soft materials to tailor viscoelastic properties for bioprinting |
CN106916781A (zh) * | 2015-12-25 | 2017-07-04 | 清华大学 | 一种体外三维人体肝组织的构建方法及其应用 |
KR20190086655A (ko) | 2016-06-17 | 2019-07-23 | 유니버시다드 데 로스 안데스 | 저온-적응된 해양생물종의 천연 공급원으로부터 유래된 젤라틴 중합체 및 그것의 용도 |
CN106589476A (zh) * | 2016-11-15 | 2017-04-26 | 广西医科大学 | 一种生物3d打印种植壳线材及其配方和制作工艺 |
EP3489314A1 (fr) * | 2017-11-23 | 2019-05-29 | Rousselot B.V. | Procédé de préparation d'hydrolysat de gélatine ayant une faible teneur en endotoxine |
-
2019
- 2019-04-03 EP EP19167094.2A patent/EP3719057A1/fr not_active Withdrawn
-
2020
- 2020-04-03 CN CN202080027214.1A patent/CN113677742A/zh active Pending
- 2020-04-03 CA CA3135934A patent/CA3135934A1/fr active Pending
- 2020-04-03 MX MX2021012139A patent/MX2021012139A/es unknown
- 2020-04-03 JP JP2021558942A patent/JP2022527533A/ja active Pending
- 2020-04-03 EP EP20715390.9A patent/EP3947529A1/fr active Pending
- 2020-04-03 US US17/491,570 patent/US20220184274A1/en active Pending
- 2020-04-03 WO PCT/EP2020/059669 patent/WO2020201555A1/fr unknown
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2021
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WO2020201555A1 (fr) | 2020-10-08 |
US20220184274A1 (en) | 2022-06-16 |
CN113677742A (zh) | 2021-11-19 |
CA3135934A1 (fr) | 2020-10-08 |
EP3719057A1 (fr) | 2020-10-07 |
MX2021012139A (es) | 2021-11-03 |
IL286899A (en) | 2021-10-31 |
JP2022527533A (ja) | 2022-06-02 |
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